Page last updated: 2024-10-18

glycine and Chronic Progressive External Ophthalmoplegia

glycine has been researched along with Chronic Progressive External Ophthalmoplegia in 2 studies

Research Excerpts

ExcerptRelevanceReference
"Autosomal dominant progressive external ophthalmoplegia is a mitochondrial disorder characterized by multiple large deletions of mitochondrial DNA."1.31A novel D104G mutation in the adenine nucleotide translocator 1 gene in autosomal dominant progressive external ophthalmoplegia patients with mitochondrial DNA with multiple deletions. ( Fukazawa, T; Goto, Y; Houzen, H; Komaki, H; Nonaka, I; Yoshida, K, 2002)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Komaki, H1
Fukazawa, T1
Houzen, H1
Yoshida, K1
Nonaka, I1
Goto, Y1
Graziewicz, MA1
Longley, MJ1
Bienstock, RJ1
Zeviani, M1
Copeland, WC1

Other Studies

2 other studies available for glycine and Chronic Progressive External Ophthalmoplegia

ArticleYear
A novel D104G mutation in the adenine nucleotide translocator 1 gene in autosomal dominant progressive external ophthalmoplegia patients with mitochondrial DNA with multiple deletions.
    Annals of neurology, 2002, Volume: 51, Issue:5

    Topics: Adult; Aged; Amino Acid Sequence; Aspartic Acid; DNA, Mitochondrial; Female; Gene Deletion; Genes, D

2002
Structure-function defects of human mitochondrial DNA polymerase in autosomal dominant progressive external ophthalmoplegia.
    Nature structural & molecular biology, 2004, Volume: 11, Issue:8

    Topics: Amino Acid Motifs; Bacterial Proteins; Catalytic Domain; Crystallography, X-Ray; DNA; DNA Polymerase

2004